Novel chiral voltammetric sensor for tryptophan enantiomers based on 3-neomenthylindene as recognition element

To achieve satisfactory recognition and determination of tryptophan (TRP) enantiomers a chiral voltammetric sensor based on carbon black paste electrode (CBPE) containing Carboblack C powder and 3-neomenthylindene (NMI) chiral selector is developed in this work. A possible recognition mechanism as w...

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Veröffentlicht in:Journal of electroanalytical chemistry (Lausanne, Switzerland) Switzerland), 2021-01, Vol.880, p.114939, Article 114939
Hauptverfasser: Zagitova, L.R., Maistrenko, V.N., Yarkaeva, Yu A., Zagitov, V.V., Zilberg, R.A., Kovyazin, P.V., Parfenova, L.V.
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container_title Journal of electroanalytical chemistry (Lausanne, Switzerland)
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creator Zagitova, L.R.
Maistrenko, V.N.
Yarkaeva, Yu A.
Zagitov, V.V.
Zilberg, R.A.
Kovyazin, P.V.
Parfenova, L.V.
description To achieve satisfactory recognition and determination of tryptophan (TRP) enantiomers a chiral voltammetric sensor based on carbon black paste electrode (CBPE) containing Carboblack C powder and 3-neomenthylindene (NMI) chiral selector is developed in this work. A possible recognition mechanism as well as chiral selectivity have been explained using the molecular dynamics simulation. It was shown that 3-neomenthylindene attracts to TRP enantiomers via Van der Waals and π-π-stacking interactions. Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP with a selectivity coefficient of 1.34. The higher response signal of L-TRP than D-TRP is due to the energetically more favorable interaction of 3-neomenthylindene with L-TRP, which is confirmed by a change in the total energy of the system. CBPE modified by NMI was characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT-IR). The electrochemical and analytical characteristics of the sensor and conditions of the voltammogram registration were studied by differential pulse voltammetry (DPV). It was found that the oxidation of TRP enantiomers on CBPE/NMI is the diffusion-controlled process. The experimental results indicate a linear correlation between the peak currents of TRP enantiomers and their concentration in the range from 2.5 μM to 0.3 mM, leading to a detection limit of 1.71 μM and 2.23 μM for L- and D-TRP, respectively. The practical capabilities of the proposed sensor were demonstrated by analyzing human urine and blood plasma with satisfactory recoveries ranging from 95.2% to 99.0%. L-TRP was recognized in dietary supplements using projection to latent structures discriminant analysis. The present sensor also can detect the enantiomeric composition based on current signals with the different total concentrations of the mixture. The selectivity, stability, and reproducibility of the proposed sensor were studied as well. [Display omitted] •A chiral sensor based on CBPE modified by 3-neomenthylindene (NMI) was developed.•Large differences in energy between π-π-stacking of NMI with L-, D-TRP were observed.•Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP.•The sensor correctly determined L- and D-TRP in real objects and enantiomeric mixture.•The recognition of L-TRP based dietary supplements using PLS-DA was successful.
doi_str_mv 10.1016/j.jelechem.2020.114939
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A possible recognition mechanism as well as chiral selectivity have been explained using the molecular dynamics simulation. It was shown that 3-neomenthylindene attracts to TRP enantiomers via Van der Waals and π-π-stacking interactions. Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP with a selectivity coefficient of 1.34. The higher response signal of L-TRP than D-TRP is due to the energetically more favorable interaction of 3-neomenthylindene with L-TRP, which is confirmed by a change in the total energy of the system. CBPE modified by NMI was characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT-IR). The electrochemical and analytical characteristics of the sensor and conditions of the voltammogram registration were studied by differential pulse voltammetry (DPV). It was found that the oxidation of TRP enantiomers on CBPE/NMI is the diffusion-controlled process. The experimental results indicate a linear correlation between the peak currents of TRP enantiomers and their concentration in the range from 2.5 μM to 0.3 mM, leading to a detection limit of 1.71 μM and 2.23 μM for L- and D-TRP, respectively. The practical capabilities of the proposed sensor were demonstrated by analyzing human urine and blood plasma with satisfactory recoveries ranging from 95.2% to 99.0%. L-TRP was recognized in dietary supplements using projection to latent structures discriminant analysis. The present sensor also can detect the enantiomeric composition based on current signals with the different total concentrations of the mixture. The selectivity, stability, and reproducibility of the proposed sensor were studied as well. [Display omitted] •A chiral sensor based on CBPE modified by 3-neomenthylindene (NMI) was developed.•Large differences in energy between π-π-stacking of NMI with L-, D-TRP were observed.•Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP.•The sensor correctly determined L- and D-TRP in real objects and enantiomeric mixture.•The recognition of L-TRP based dietary supplements using PLS-DA was successful.</description><identifier>ISSN: 1572-6657</identifier><identifier>EISSN: 1873-2569</identifier><identifier>DOI: 10.1016/j.jelechem.2020.114939</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>3-Neomenthylindene ; Blood plasma ; Carbon black ; Carbon black paste electrode ; Chiral sensor ; Discriminant analysis ; Electrochemical impedance spectroscopy ; Enantiomers ; Fourier transforms ; Infrared analysis ; Infrared spectroscopy ; Molecular dynamics ; Oxidation ; Recognition ; Selectivity ; Sensors ; Spectrum analysis ; Tryptophan ; Tryptophan enantiomers ; Voltammetry ; π-π-stacking</subject><ispartof>Journal of electroanalytical chemistry (Lausanne, Switzerland), 2021-01, Vol.880, p.114939, Article 114939</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. 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A possible recognition mechanism as well as chiral selectivity have been explained using the molecular dynamics simulation. It was shown that 3-neomenthylindene attracts to TRP enantiomers via Van der Waals and π-π-stacking interactions. Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP with a selectivity coefficient of 1.34. The higher response signal of L-TRP than D-TRP is due to the energetically more favorable interaction of 3-neomenthylindene with L-TRP, which is confirmed by a change in the total energy of the system. CBPE modified by NMI was characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT-IR). The electrochemical and analytical characteristics of the sensor and conditions of the voltammogram registration were studied by differential pulse voltammetry (DPV). It was found that the oxidation of TRP enantiomers on CBPE/NMI is the diffusion-controlled process. The experimental results indicate a linear correlation between the peak currents of TRP enantiomers and their concentration in the range from 2.5 μM to 0.3 mM, leading to a detection limit of 1.71 μM and 2.23 μM for L- and D-TRP, respectively. The practical capabilities of the proposed sensor were demonstrated by analyzing human urine and blood plasma with satisfactory recoveries ranging from 95.2% to 99.0%. L-TRP was recognized in dietary supplements using projection to latent structures discriminant analysis. The present sensor also can detect the enantiomeric composition based on current signals with the different total concentrations of the mixture. The selectivity, stability, and reproducibility of the proposed sensor were studied as well. [Display omitted] •A chiral sensor based on CBPE modified by 3-neomenthylindene (NMI) was developed.•Large differences in energy between π-π-stacking of NMI with L-, D-TRP were observed.•Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP.•The sensor correctly determined L- and D-TRP in real objects and enantiomeric mixture.•The recognition of L-TRP based dietary supplements using PLS-DA was successful.</description><subject>3-Neomenthylindene</subject><subject>Blood plasma</subject><subject>Carbon black</subject><subject>Carbon black paste electrode</subject><subject>Chiral sensor</subject><subject>Discriminant analysis</subject><subject>Electrochemical impedance spectroscopy</subject><subject>Enantiomers</subject><subject>Fourier transforms</subject><subject>Infrared analysis</subject><subject>Infrared spectroscopy</subject><subject>Molecular dynamics</subject><subject>Oxidation</subject><subject>Recognition</subject><subject>Selectivity</subject><subject>Sensors</subject><subject>Spectrum analysis</subject><subject>Tryptophan</subject><subject>Tryptophan enantiomers</subject><subject>Voltammetry</subject><subject>π-π-stacking</subject><issn>1572-6657</issn><issn>1873-2569</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFUE1LxDAQLaLguvoXJOC5a5I2aXpTFr9g0YueQzaZuiltUpO4sP_eLNWzh2GGN--9YV5RXBO8Ipjw237VwwB6B-OKYppBUrdVe1IsiGiqkjLenuaZNbTknDXnxUWMPcZUCEIXhXv1exiQ3tmgBrT3Q1LjCClYjSK46APqcqVwmJKfdsohcMol60cIEW1VBIO8Q1XpIEMu7Q6DdQYcIBVRAO0_nc3sLBvguL8szjo1RLj67cvi4_Hhff1cbt6eXtb3m1JXNU4loUprChz0ltdUbImqtDGcEa6FqgXdNpwpzYzGraYdqZkgGJuWUtOBYNBVy-Jm9p2C__qGmGTvv4PLJyWt24YSIVidWXxm6eBjDNDJKdhRhYMkWB6zlb38y1Yes5Vztll4Nwsh_7C3EGTUFpwGY_PTSRpv_7P4Ad8HiKI</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Zagitova, L.R.</creator><creator>Maistrenko, V.N.</creator><creator>Yarkaeva, Yu A.</creator><creator>Zagitov, V.V.</creator><creator>Zilberg, R.A.</creator><creator>Kovyazin, P.V.</creator><creator>Parfenova, L.V.</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20210101</creationdate><title>Novel chiral voltammetric sensor for tryptophan enantiomers based on 3-neomenthylindene as recognition element</title><author>Zagitova, L.R. ; 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A possible recognition mechanism as well as chiral selectivity have been explained using the molecular dynamics simulation. It was shown that 3-neomenthylindene attracts to TRP enantiomers via Van der Waals and π-π-stacking interactions. Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP with a selectivity coefficient of 1.34. The higher response signal of L-TRP than D-TRP is due to the energetically more favorable interaction of 3-neomenthylindene with L-TRP, which is confirmed by a change in the total energy of the system. CBPE modified by NMI was characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT-IR). The electrochemical and analytical characteristics of the sensor and conditions of the voltammogram registration were studied by differential pulse voltammetry (DPV). It was found that the oxidation of TRP enantiomers on CBPE/NMI is the diffusion-controlled process. The experimental results indicate a linear correlation between the peak currents of TRP enantiomers and their concentration in the range from 2.5 μM to 0.3 mM, leading to a detection limit of 1.71 μM and 2.23 μM for L- and D-TRP, respectively. The practical capabilities of the proposed sensor were demonstrated by analyzing human urine and blood plasma with satisfactory recoveries ranging from 95.2% to 99.0%. L-TRP was recognized in dietary supplements using projection to latent structures discriminant analysis. The present sensor also can detect the enantiomeric composition based on current signals with the different total concentrations of the mixture. The selectivity, stability, and reproducibility of the proposed sensor were studied as well. [Display omitted] •A chiral sensor based on CBPE modified by 3-neomenthylindene (NMI) was developed.•Large differences in energy between π-π-stacking of NMI with L-, D-TRP were observed.•Compared with D-TRP, the sensor indicates favorable chiral recognition towards L-TRP.•The sensor correctly determined L- and D-TRP in real objects and enantiomeric mixture.•The recognition of L-TRP based dietary supplements using PLS-DA was successful.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jelechem.2020.114939</doi></addata></record>
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subjects 3-Neomenthylindene
Blood plasma
Carbon black
Carbon black paste electrode
Chiral sensor
Discriminant analysis
Electrochemical impedance spectroscopy
Enantiomers
Fourier transforms
Infrared analysis
Infrared spectroscopy
Molecular dynamics
Oxidation
Recognition
Selectivity
Sensors
Spectrum analysis
Tryptophan
Tryptophan enantiomers
Voltammetry
π-π-stacking
title Novel chiral voltammetric sensor for tryptophan enantiomers based on 3-neomenthylindene as recognition element
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